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Sialolithiasis (PheCode 528.7)

WARS2 · rs183191767

What the study found

Who was studied 248 African American or Afro-Caribbean cases, 121,451 African American or Afro-Caribbean controls, 449 European ancestry cases, 450,273 European ancestry controls.

The effect Each copy of the C allele shifted the measure 3.42 lower (95% confidence interval 3.4-3.44); p = 1 × 10−13.

How common The C allele had a frequency of about 100% in the people studied.

Where it sits Chromosome 1, band 1p12 — in an intron of WARS2.

What each result means

C/C Two copies of the version the research linked to Sialolithiasis (PheCode 528.7). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Sialolithiasis (PheCode 528.7). That is a smaller link than two copies.
T/T No copy of the version the research linked to Sialolithiasis (PheCode 528.7). This is the starting point the study compared everyone against.
Source

Questions about rs183191767

What is rs183191767?

rs183191767 is a single position in the genome, in or near the WARS2 gene. Published research associates it with sialolithiasis (phecode 528.7). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs183191767 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs183191767 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Sialolithiasis (PheCode 528.7) (rs183191767). MyGeneLog™. https://www.mygenelog.com/variants/rs183191767

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